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Volume 37, Issue 1, Pages 40-47 (January 2006)


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A proposal for a new validated histological definition of the gastroesophageal junction

Parakrama Chandrasoma, MDCorresponding Author Informationemail address, Kathleen Makarewicz, MD, Kumari Wickramasinghe, MD, Yanling Ma, MD, Tom Demeester, MD

Received 16 June 2005; received in revised form 4 September 2005; accepted 8 September 2005. published online 28 November 2005.

Summary 

Present definitions of the gastroesophageal junction (GEJ) are the point of flaring of the tubular esophagus and the proximal limit of the gastric rugal folds. Neither of these has been validated as the true GEJ. This study aims to validate the location of the true GEJ using the criterion of esophageal submucosal glands. Ten esophagogastrectomy specimens, in which there was a well-defined point of flaring of the tubular esophagus that coincided with the proximal limit of gastric rugal folds, were examined by complete histological mapping to evaluate the distribution of esophageal submucosal glands and surface epithelial types. Oxyntocardiac and cardiac mucosa with or without intestinal metaplasia were present under rugal folds distal to the end of tubular esophagus in all patients to a length of 0.31 to 2.05 cm. Submucosal glands were present in the tubular esophagus and in the proximal pouch distal to the tubular esophagus in a distribution that closely coincided with squamous epithelium, oxyntocardiac, cardiac, and intestinal epithelia. Submucosal glands were never found under oxyntic mucosa. We conclude that a variable part of the saccular region distal to the tubular esophagus contains esophageal submucosal glands, therefore representing reflux-damaged distal esophagus. This results in an error, where up to 2.05 cm of distal reflux-damaged dilated esophagus can be mistaken as proximal stomach when presently accepted definitions for the GEJ are used. The true GEJ is the proximal limit of gastric oxyntic mucosa defined by histology.

Department of Surgical Pathology and Foregut Surgery (TDM), Keck School of Medicine, University of Southern California, Los Angeles, CA, USA

Corresponding Author InformationCorresponding author. Department of Surgical Pathology, LAC+USC Medical Center, Los Angeles, CA 90033, USA.

 This study has no external funding source.

PII: S0046-8177(05)00522-8

doi:10.1016/j.humpath.2005.09.019


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